均苯四甲酰亚胺桥联的聚酞菁亚铁的氧还原反应(英文)  

Oxygen-Reduction Reaction of Pyromellitimide-Bridged Polyphthalocyanine Fe(Ⅱ)

作　　者：孙晓然[1,2] 李光跃[2] 夏定国[3] 张立美[2] 李钒[1] 

机构地区：[1]北京工业大学化学与环境工程学院,北京100086 [2]河北联合大学化学工程学院,河北唐山063009 [3]北京大学工学院,北京100871

出　　处：《物理化学学报》2013年第7期1461-1466,共6页Acta Physico-Chimica Sinica

基　　金：supported by the National Natural Science Foundation of China (11247281);Beijing Natural Science Foundation, China (2120001);Excellent Youth Fund of Hebei Province Department of Education, China (Y2012010)~~

摘　　要：用密度泛函方法研究了一种均苯四甲酰亚胺桥联的聚酞菁亚铁的氧还原反应.设计了三个模型分子以研究此催化剂在不同聚合度时的氧还原催化反应性能.使用BP86泛函和SVP基组进行构型优化得到模型分子及其氧气复合物的电子和分子结构.此催化剂中心的铁原子和氧气以双键结合并发生电荷转移时,氧气被还原.这证明此催化剂具有良好的催化氧还原能力.通过前沿轨道分析以及模型分子氧气复合物稳定性分析证实,具有较高聚合度和较强吸电子取代基的催化剂具有更好的氧还原活性.催化剂的催化性能通过一个电催化循环来实现.在此循环过程中,氧气结合氢离子被还原为水,因此此催化剂需要在酸性介质中使用.The activity of a pyromellitimide-bridged polyphthalocyanine Fe（ll） catalyst for 02 reduction is studied by density functional theory calculations. Three model molecules with different polymerization degrees are designed to investigate O2-reduction electrocatalytic reactivity. The molecular and electronic structures of the models and their O2-complexes are optimized with BP86 functional and SVP basis sets. The central Fe atom in the catalyst binds 02 by a double bond followed by a charge transfer to reduce 02. This study indicates that the catalyst has potential for O2-reduction electrocatalytic activity. The calculated frontier molecular orbitals and stabilities of the O2-complexes demonstrate that catalysts with a higher polymerization degree and stronger electron-withdrawing groups will have higher activities for 02 reduction. O2-reduction activity of the catalyst is achieved via an electrocatalytic cycle.

关 键 词：聚酞菁 铁 氧还原 反应性 密度泛函理论 

分 类 号：O621.254[理学—有机化学]